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The Health Sciences Authority (HSA) in Singapore has a post-market surveillance program to monitor the quality, safety, and efficacy of therapeutic products. A crucial part of this program is managing product defects. As a product registrant, manufacturer, importer, or supplier, you must report any defects related to your therapeutic products to the HSA and notify them before recalling any product. This video provides essential information on the requirements and processes for defect reporting and product recalls. Defects may occur during manufacturing, storage, and handling of products, and it's vital to report these, especially if they impact safety, quality, or efficacy, to protect public health.